Pharmaceutical Manufacturing Technician

SAFC•Verona, WI

6d•Onsite

About The Position

This role is for a Pharmaceutical Manufacturing Technician at MilliporeSigma. The technician will be responsible for following and promoting safety protocols, maintaining the cleanliness and safety of production areas and equipment, especially when handling potent compounds. They will work with written procedures, operate production equipment for cGMP production of APIs and intermediates, and communicate production status. The role involves correcting safety and process issues, participating in a team-based, multi-shift environment, and providing departmental support. Responsibilities also include identifying and correcting equipment, process, and safety issues, verifying material and equipment quality, updating batch records and computer systems (including SAP), and maintaining lab housekeeping. The position has a strategic impact on safety, quality, operational excellence, skill development, and regulatory compliance.

Requirements

High School Diploma or GED
2+ years of experience in a chemical manufacturing or analytical lab
Ability to read and understand written protocols
Basic computer literacy (Microsoft Word, PowerPoint, Email, etc.)
Strong problem-solving skills
Effective oral and written communication skills
Mechanical and technical aptitude; able to operate hand tools, calculators, and weighing/measuring devices
Basic mathematical skills
High degree of motivation and self-starter attitude
Ability to multi-task while paying close attention to detail
Able to stand for long periods in full PEE
Lift and move up to 50 pounds throughout the shift
Experience working with highly potent/hazardous materials and understanding chemical hazards
Ability to work in Class 1 / Div 2 areas and near moving mechanical parts

Responsibilities

Consistently follow and actively promote proper safety protocols and PPE to other staff.
Maintain the safety and cleanliness of production areas and all related equipment, specifically focusing on potent compound handling techniques.
Utilize a variety of written procedures, including batch records and existing operating procedures.
Function as a primary or secondary operator for cGMP production of APIs and intermediates.
Effectively operate production equipment during production, cleaning, and maintenance to support operations.
Communicate production status effectively through shift pass-off tools and various computer systems.
Correct safety and process issues identified through standard inspections and audits in a timely manner.
Participate in a team-based, multi-shift manufacturing environment.
Provide departmental support through additional tasks as directed by leadership and take ownership of departmental responsibilities.
Help identify and correct equipment, process, and safety issues in the lab.
Verify the quality and integrity of materials and equipment.
Update batch records, computer systems, including SAP, according to procedures.
Maintain high-quality in-lab housekeeping.